Exploring the Ability of Cyclic Peptides to Target SAM Domains: A Computational and Experimental Study.

Abstract

Sterile alpha motif (SAM) domains are protein interaction modules with a helical fold. SAM-SAM interactions often adopt the mid-loop (ML)/end-helix (EH) model, in which the C-terminal helix and adjacent loops of one SAM unit (EH site) bind the central regions of another SAM domain (ML site). Herein, an original strategy to attack SAM-SAM associations is reported. It relies on the design of cyclic peptides that target a region of the SAM domain positioned at the bottom side of the EH interface, which is thought to be important for the formation of a SAM-SAM complex. This strategy has been preliminarily tested by using a model system of heterotypic SAM-SAM interactions involving the erythropoietin-producing hepatoma kinase A2 (EphA2) receptor and implementing a multidisciplinary plan made up of computational docking studies, experimental interaction assays (by NMR spectroscopy and surface plasmon resonance techniques) and conformational analysis (by NMR spectroscopy and circular dichroism). This work further highlights how only a specific balance between flexibility and rigidity may be needed to generate modulators of SAM-SAM interactions.

• Authors: Flavia A Mercurio, Concetta Di Natale, Luciano Pirone, Marian Vincenzi, Daniela Marasco, Stefania De Luca, Emilia M Pedone, Marilisa Leone
• Journal: Chembiochem : a European journal of chemical biology (Chembiochem) Vol. 21 Issue 5 Pg. 702-711 (03 02 2020) ISSN: 1439-7633 [Electronic] Germany
• PMID: 31538690 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Chemical References

• Peptide Library
• Peptides, Cyclic
• Receptor, EphA2

Topics

• Humans
• Molecular Docking Simulation
• Peptide Library
• Peptides, Cyclic (chemistry, metabolism)
• Protein Binding
• Protein Conformation
• Receptor, EphA2 (metabolism)
• Sterile Alpha Motif